HRID352264

反应详情

EQUATION

反应方程式

HRID 352264 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

A mixture consisting of 4-bromophenol (20.75 g), 6-chloro-1-hexanol (20.50 g), potassium carbonate (33.20 g) and potassium iodide (21.9 g) in dimethylsulfoxide was stirred for 6 hours at 80° C. The reaction mixture was cooled and poured into 500 ml of water and extracted with 2×500 ml of ethyl acetate. The combined organic extracts were washed with saturated NaCl solution (3×100 ml) dried over magnesium sulfate and evaporated to dryness. This gave 37.4 g of a slightly beige oil of which 24.9 g were dissolved in 250 ml of dichloromethane containing 8.05 g of 3.4-didydro-2H-pyran. The resulting solution was cooled to 5° C. A solution of bis-trimethylsilyl sulfate (0.38 g) in 10 ml of dichloromethane was then added dropwise to the reaction mixture. The resulting mixture was stirred for two hours at 5° C. Triethylamine (4 ml) was added to the reaction mixture and stirring was continued for one hour at room temperature. The reaction mixture was then poured into 300 ml of water and extracted with dichloromethane (2×300 ml). The combined organic extracts were dried over magnesium sulfate and evaporated to dryness to give 33.95 g of a slightly beige residue, which was then filtered through a silica gel column using a cyclohexane/ethyl acetate (8/2) as eluent to give 28.9 g of 4-bromo-1-[6-(tetrahydropyran-2-yloxy)hexyloxy]benzene as colourless oil.

WORKUP

后处理

  1. temperatureThe reaction mixture was cooled
  2. extractionextracted with 2×500 ml of ethyl acetate
  3. washThe combined organic extracts were washed with saturated NaCl solution (3×100 ml)
  4. dry with materialdried over magnesium sulfate
  5. customevaporated to dryness
  6. dissolutionThis gave 37.4 g of a slightly beige oil of which 24.9 g were dissolved in 250 ml of dichloromethane containing 8.05 g of 3
  7. temperatureThe resulting solution was cooled to 5° C
  8. additionA solution of bis-trimethylsilyl sulfate (0.38 g) in 10 ml of dichloromethane was then added dropwise to the reaction mixture
  9. stirringThe resulting mixture was stirred for two hours at 5° C
  10. additionTriethylamine (4 ml) was added to the reaction mixture
  11. stirringstirring
  12. waitwas continued for one hour at room temperature
  13. additionThe reaction mixture was then poured into 300 ml of water
  14. extractionextracted with dichloromethane (2×300 ml)
  15. dry with materialThe combined organic extracts were dried over magnesium sulfate
  16. customevaporated to dryness
  17. customto give 33.95 g of a slightly beige residue, which
  18. filtrationwas then filtered through a silica gel column